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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148239copy number variation1nstd102humanPathogenic GRCh38 chr13: 98,343,655-110,990,677 , GRCh37.p13 chr13: 98,995,909-111,643,024 CLYBL-AS3, PPIAP24, 162 more genes
    nsv7148164copy number variation1nstd102humanPathogenic GRCh38 chr13: 106,425,676-114,326,445 , GRCh37.p13 chr13: 107,078,024-115,085,141 TUBGCP3, LINC01043, 132 more genes
    nsv7062466inversion1nstd229human GRCh38 chr13: 107,288,249-110,580,799 , GRCh37.p13 chr13: 107,940,597-111,233,146 RNA5SP39, MIR1267, 32 more genes
    nsv7060236inversion1nstd229human GRCh38 chr13: 109,400,177-111,221,158 , GRCh37.p13 chr13: 110,052,524-111,873,505 LINC00399, ANKRD10, 36 more genes
    nsv6955804copy number variation1nstd229human GRCh38 chr13: 109,727,989-109,728,157 , GRCh37.p13 chr13: 110,380,336-110,380,504 LINC00676
    nsv6955419copy number variation1nstd229human GRCh38 chr13: 109,720,220-109,728,641 , GRCh37.p13 chr13: 110,372,567-110,380,988 LINC00676
    nsv6954531copy number variation1nstd229human GRCh38 chr13: 109,465,901-109,921,000 , GRCh37.p13 chr13: 110,118,248-110,573,347 LOC101927627, RN7SKP10, 4 more genes
    nsv6951411copy number variation1nstd229human GRCh38 chr13: 107,488,002-110,580,394 , GRCh37.p13 chr13: 108,140,350-111,232,741 LOC105370359, RN7SKP10, 30 more genes
    nsv6948278copy number variation1nstd229human GRCh38 chr13: 109,726,038-109,755,555 , GRCh37.p13 chr13: 110,378,385-110,407,902 LINC00676, IRS2
    nsv6939499copy number variation1nstd229human GRCh38 chr13: 109,704,784-109,734,262 , GRCh37.p13 chr13: 110,357,131-110,386,609 LINC00676
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637531copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,334,135-110,383,902 , GRCh38.p12 chr13: 99,681,881-109,731,555 ARGLU1, LINC00343, 101 more genes
    nsv6637400copy number variation1nstd102humanPathogenic GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258 LOC107984609, LINC00354, 265 more genes
    nsv6637217copy number variation1nstd102humanPathogenic GRCh37 chr13: 99,421,603-115,107,733 , GRCh38.p12 chr13: 98,769,349-114,342,258 LOC107984609, CLYBL-AS2, 231 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6621646copy number variation1nstd224human GRCh37 chr13: 110,371,264-110,482,739 , GRCh38.p12 chr13: 109,718,917-109,830,392 IRS2, LINC00676, 1 more genes
    nsv6621645copy number variation1nstd224human GRCh37 chr13: 110,236,646-115,091,330 , GRCh38.p12 chr13: 109,584,299-114,325,855 PARP1P1, F7, 103 more genes
    nsv6487881copy number variation1nstd223human GRCh38 chr13: 109,704,782-109,734,274 , GRCh37.p13 chr13: 110,357,129-110,386,621 LINC00676
    nsv6487463copy number variation1nstd223human GRCh38 chr13: 109,551,901-109,922,600 , GRCh37.p13 chr13: 110,204,248-110,574,947 LOC107984602, RN7SKP10, 4 more genes
    nsv6487192copy number variation1nstd223human GRCh38 chr13: 109,701,701-109,828,300 , GRCh37.p13 chr13: 110,354,048-110,480,647 LINC00676, LOC105370360, 1 more genes
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